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Aromatic L-Amino acid decarboxylase deficiency: A new case from Turkey with a novel mutation

Aromatic L-amino acid decarboxylase (AADC), a vitamin B6-requiring enzyme that converts L-dopa to dopamine and 5-hydroxytryptophan to serotonin. Deficiency of this enzyme results in developmental delay, muscular hypotonia, dystonia, involuntary movements, autonomic dysfunction, and oculogyric crises...

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Autores principales: Gücüyener, Kıvılcım, Kasapkara, Çiğdem Seher, Tümer, Leyla, Verbeek, Marcel M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4090859/
https://www.ncbi.nlm.nih.gov/pubmed/25024584
http://dx.doi.org/10.4103/0972-2327.132652
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author Gücüyener, Kıvılcım
Kasapkara, Çiğdem Seher
Tümer, Leyla
Verbeek, Marcel M.
author_facet Gücüyener, Kıvılcım
Kasapkara, Çiğdem Seher
Tümer, Leyla
Verbeek, Marcel M.
author_sort Gücüyener, Kıvılcım
collection PubMed
description Aromatic L-amino acid decarboxylase (AADC), a vitamin B6-requiring enzyme that converts L-dopa to dopamine and 5-hydroxytryptophan to serotonin. Deficiency of this enzyme results in developmental delay, muscular hypotonia, dystonia, involuntary movements, autonomic dysfunction, and oculogyric crises. We now report a 2-year-old Turkish boy with AADC deficiency confirmed by greatly reduced AADC activity in the plasma and by genetic studies. Mutation analysis revealed a homozygous mutation c.208C > T (p. His70Tyr) in exon 3 of the AADC gene which has not been described to date.
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spelling pubmed-40908592014-07-14 Aromatic L-Amino acid decarboxylase deficiency: A new case from Turkey with a novel mutation Gücüyener, Kıvılcım Kasapkara, Çiğdem Seher Tümer, Leyla Verbeek, Marcel M. Ann Indian Acad Neurol Case Report Aromatic L-amino acid decarboxylase (AADC), a vitamin B6-requiring enzyme that converts L-dopa to dopamine and 5-hydroxytryptophan to serotonin. Deficiency of this enzyme results in developmental delay, muscular hypotonia, dystonia, involuntary movements, autonomic dysfunction, and oculogyric crises. We now report a 2-year-old Turkish boy with AADC deficiency confirmed by greatly reduced AADC activity in the plasma and by genetic studies. Mutation analysis revealed a homozygous mutation c.208C > T (p. His70Tyr) in exon 3 of the AADC gene which has not been described to date. Medknow Publications & Media Pvt Ltd 2014 /pmc/articles/PMC4090859/ /pubmed/25024584 http://dx.doi.org/10.4103/0972-2327.132652 Text en Copyright: © Annals of Indian Academy of Neurology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Gücüyener, Kıvılcım
Kasapkara, Çiğdem Seher
Tümer, Leyla
Verbeek, Marcel M.
Aromatic L-Amino acid decarboxylase deficiency: A new case from Turkey with a novel mutation
title Aromatic L-Amino acid decarboxylase deficiency: A new case from Turkey with a novel mutation
title_full Aromatic L-Amino acid decarboxylase deficiency: A new case from Turkey with a novel mutation
title_fullStr Aromatic L-Amino acid decarboxylase deficiency: A new case from Turkey with a novel mutation
title_full_unstemmed Aromatic L-Amino acid decarboxylase deficiency: A new case from Turkey with a novel mutation
title_short Aromatic L-Amino acid decarboxylase deficiency: A new case from Turkey with a novel mutation
title_sort aromatic l-amino acid decarboxylase deficiency: a new case from turkey with a novel mutation
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4090859/
https://www.ncbi.nlm.nih.gov/pubmed/25024584
http://dx.doi.org/10.4103/0972-2327.132652
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AT tumerleyla aromaticlaminoaciddecarboxylasedeficiencyanewcasefromturkeywithanovelmutation
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